Search for a gene
AGL - amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
- Synonym(s) : GDE, glycogen debranching enzyme, glycogen storage disease type III
- Previous symbols and names : amylo-1, 6-glucosidase, 4-alpha-glucanotransferase
- Type : gene with protein product
- Chromosomal location : 1p21.2
- OMIM: 610860
- HGNC: 321
- UniProtKB: P35573
- Genatlas: AGL
- GenCC: AGL
- Ensembl: ENSG00000162688
- IUPHAR-DB: -
- Reactome: P35573
- LOVD: AGL
Diseases list
- Disease-causing germline mutation(s) in Glycogen storage disease due to glycogen debranching enzyme deficiency
ORPHA:366 
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources.